Idevax launches a series of short movies. Part 3 is all about challenges and opportunities seen with the Medical Device Regulations (MDR). These also impact Idevax and the VAX-ID device.
Meet our Quality Assurance and Regulatory Affairs Manager, Daniele Scalco Vasconcelos.
She highlights the impact of the regulations, its strengths and weaknesses. Also, she explains how medical device manufacturers can implement the MDR requirements successfully based on her master thesis and professional experience.